Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs144567652
rs144567652
0.010 GeneticVariation BEFREE As further evidence, we detected two additional NOA-affected case subjects with independent FANCM homozygous nonsense variants, one from Estonia (p.Gln1701<sup>∗</sup>; rs147021911) and another from Portugal (p.Arg1931<sup>∗</sup>; rs144567652). 30075111

2018